Catalog Number

33551

Brand Name

Kendall

Version/Model Number

33551

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

IKD

Product Code Name

CABLE, ELECTRODE

Public Device Record Key

de9bdf96-6de2-40e6-9fc0-1afb685b5dd7

Public Version Date

March 25, 2019

Public Version Number

1

DI Record Publish Date

March 15, 2019

Package DI Number

50885380166219

Quantity per Package

12

Contains DI Package

10885380166211

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE